SCHEMBL4833392

SCHEMBL4833392

O=C(CO)c1ccc(-c2ccccc2)cc1

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 5/20 0.67
MAPT P10636 5/20 0.67
L3MBTL1 Q9Y468 2/20 0.67
PTPN1 P18031 1/20 0.67
GSK3B P49841 1/20 0.67
RAB9A P51151 4/20 0.64
FFAR1 O14842 1/20 0.64
LMNA P02545 1/20 0.64
CYP1A2 P05177 1/20 0.64
HIF1A Q16665 1/20 0.64
HPGD P15428 2/20 0.62
ERCC5 P28715 1/20 0.62
FEN1 P39748 1/20 0.62
HAO1 Q9UJM8 1/20 0.62
ALDH1A1 P00352 4/20 0.60
KDM4E B2RXH2 3/20 0.60
USP2 O75604 1/20 0.60
AGTR1 P30556 1/20 0.56
SRD5A2 P31213 1/20 0.55
NPC1 O15118 2/20 0.52

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Benzene SCHEMBL27878545 0.85 TDP1 (0.67) SMN1; SMN2MAPTL3MBTL1PTPN1GSK3B
SCHEMBL27431671 0.85 TDP1 (0.67) SMN1; SMN2MAPTL3MBTL1PTPN1GSK3B
SCHEMBL44898 0.85 TDP1 (0.67) SMN1; SMN2MAPTL3MBTL1PTPN1GSK3B
SCHEMBL11868666 0.85 TDP1 (0.67) SMN1; SMN2MAPTL3MBTL1PTPN1GSK3B
SCHEMBL27182280 0.84 ERCC5 (0.77) SMN1; SMN2MAPTL3MBTL1PTPN1GSK3B
SCHEMBL11410208 0.83 TDP1 (0.64) SMN1; SMN2MAPTL3MBTL1PTPN1GSK3B
Methane SCHEMBL506260 0.83 TDP1 (0.64) SMN1; SMN2MAPTL3MBTL1PTPN1GSK3B
SCHEMBL10595732 0.83 TDP1 (0.64) SMN1; SMN2MAPTL3MBTL1PTPN1GSK3B
Hydrogen Sulfide SCHEMBL843971 0.83 TDP1 (0.64) SMN1; SMN2MAPTL3MBTL1PTPN1GSK3B
SCHEMBL3639678 0.83 TDP1 (0.64) SMN1; SMN2MAPTL3MBTL1PTPN1GSK3B

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 42 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109678788-B 1, 2-diaryl indole, derivative and synthetic method thereof 湘潭大学 2021-05-04 CN claimed
CN-109678788-A A kind of 1,2- diaryl indoles, derivative and its synthetic method 湘潭大学 2019-04-26 CN claimed
US-4217360-A LUTEOLYTIC SCHERING AKTIENGESELLSCHAFT (DE) 1980-08-12 US claimed
US-20240198581-A2 Parallelized 3D Lithography Using Multi-Beam, Multi-Color Light-Induced Polymerization Karlsruher Institut für Technologie (DE) 2024-06-20 US disclosed
US-11999098-B2 Parallelized 3D lithography using multi-beam, multi-color light-induced polymerization Karlsruher Institut für Technologie (DE) 2024-06-04 US disclosed
US-20220055290-A1 Parallelized 3D Lithography Using Multi-Beam, Multi-Color Light-Induced Polymerization KARLSRUHER INST TECHNOLOGIE (DE) 2022-02-24 US disclosed
EP-3898181-A1 PARALLELISED 3D LITHOGRAPHY USING MUTI-BEAM, MULTI-COLOUR LIGHT-INDUCED POLYMERISATION Karlsruher Institut für Technologie (DE) 2021-10-27 EP disclosed
CN-109678788-B 1, 2-diaryl indole, derivative and synthetic method thereof 湘潭大学 2021-05-04 CN disclosed
US-20210008045-A1 PANICINOTAM DERIVATIVE, PREPARATION METHOD AND USE THEREOF OCEAN UNIVERSITY OF CHINA (CN) 2021-01-14 US disclosed
CN-109678788-A A kind of 1,2- diaryl indoles, derivative and its synthetic method 湘潭大学 2019-04-26 CN disclosed
CN-104177241-B Alkynyl diketone compound and synthetic method thereof 华东师范大学 2017-01-11 CN disclosed
US-4536517-A ANTIDIABETIC, ANTILIPEMIC AGENTS AMERICAN CYANAMID COMPANY (US) 1985-08-20 US disclosed
US-4307020-A REACTING AN 0-HYDROXYACETOPHENONE WITH A GLYOXYLIC ACID BAYER AKTIENGESELLSCHAFT (DE) 1981-12-22 US disclosed
US-4289887-A OPTICAL BRIGHTENERS BAYER AKTIENGESELLSCHAFT (DE) 1981-09-15 US disclosed
US-4285965-A FUNGICIDES AND INSECTICIDES FOR PLANTS BAYER AKTIENGESELLSCHAFT (DE) 1981-08-25 US disclosed
EP-0000377-B1 PROCESS FOR THE PREPARATION OF CHROMONE DERIVATIVES, NEW CHROMONE DERIVATIVES AND THEIR USE AS PLANT-PROTECTING AGENTS BAYER AG (DE) 1981-01-21 EP disclosed
EP-0019182-A1 Benzofuran derivatives and their use as optical brighteners BAYER AG (DE) 1980-11-26 EP disclosed
US-4217360-A LUTEOLYTIC SCHERING AKTIENGESELLSCHAFT (DE) 1980-08-12 US disclosed
US-4189498-A FUNGICIDES, ARTHROPODICIDES BAYER AKTIENGESELLSCHAFT (DE) 1980-02-19 US disclosed
EP-0000377-A1 Process for the preparation of chromone derivatives, new chromone derivatives and their use as plant-protecting agents BAYER AG (DE) 1979-01-24 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20210008045-A1 PANICINOTAM DERIVATIVE, PREPARATION METHOD AND USE THEREOF TPMT, PBRM1, PGM2 SMN1; SMN2 4172/4885MAPT 4/4885L3MBTL1 4171/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.